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Z Gelman-Kohan

Showing results (1-10 of 13) with videos related to

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Journal of Perinatal Medicine|January 1, 1997
Microcephaly due to fetal brain disruption sequence. Case reportL Gabis, Z Gelman-Kohan, M Mogilner
Harefuah|February 15, 1993
[Huntington's disease: ethical aspects of presymptomatic testing]Z Gelman-Kohan, J Chemke, R Nisani
Human Genetics|October 1, 1993
Homozygosity for inversion (2)(p12q14)Z Gelman-Kohan, J Rosensaft, R N Ben-Cohen, et al.
Eye (London, England)|February 29, 2000
Predictive value of family data for the management of infantile bilateral partial cataractM Oliver, A Pollack, Z Gelman-Kohan, et al.
Journal of Inherited Metabolic Disease|October 13, 1999
Transcobalamin II deficiency with methylmalonic aciduria in three sistersH Bibi, Z Gelman-Kohan, E R Baumgartner, et al.
Prenatal Diagnosis|February 1, 1996
Cytogenetic analysis of fetal chondrocytes: a comparative studyZ Gelman-Kohan, J Rosensaft, H Ben-Hur, et al.
European Journal of Pediatrics|September 1, 1991
Further delineation of the acrocallosal syndromeZ Gelman-Kohan, J Antonelli, H Ankori-Cohen, et al.
American Journal of Medical Genetics|December 1, 1994
Neurofibromatosis type I (NFI) in Israeli families: linkage analysis as a diagnostic toolS Elyakim, I Lerer, J Zlotogora, et al.
American Journal of Perinatology|March 1, 1994
Aplasia cutis congenita, elevated alpha-fetoprotein, and a distinct amniotic fluid acetylcholinesterase electrophoretic bandY Dror, Z Gelman-Kohan, Z Hagai, et al.
Journal of Medical Genetics|December 1, 1995
Familial café au lait spots: a variant of neurofibromatosis type 1D Abeliovich, Z Gelman-Kohan, S Silverstein, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Journal of Perinatal Medicine|January 1, 1997
Microcephaly due to fetal brain disruption sequence. Case reportL Gabis, Z Gelman-Kohan, M Mogilner
Harefuah|February 15, 1993
[Huntington's disease: ethical aspects of presymptomatic testing]Z Gelman-Kohan, J Chemke, R Nisani
Human Genetics|October 1, 1993
Homozygosity for inversion (2)(p12q14)Z Gelman-Kohan, J Rosensaft, R N Ben-Cohen, et al.
Eye (London, England)|February 29, 2000
Predictive value of family data for the management of infantile bilateral partial cataractM Oliver, A Pollack, Z Gelman-Kohan, et al.
Journal of Inherited Metabolic Disease|October 13, 1999
Transcobalamin II deficiency with methylmalonic aciduria in three sistersH Bibi, Z Gelman-Kohan, E R Baumgartner, et al.
Prenatal Diagnosis|February 1, 1996
Cytogenetic analysis of fetal chondrocytes: a comparative studyZ Gelman-Kohan, J Rosensaft, H Ben-Hur, et al.
European Journal of Pediatrics|September 1, 1991
Further delineation of the acrocallosal syndromeZ Gelman-Kohan, J Antonelli, H Ankori-Cohen, et al.
American Journal of Medical Genetics|December 1, 1994
Neurofibromatosis type I (NFI) in Israeli families: linkage analysis as a diagnostic toolS Elyakim, I Lerer, J Zlotogora, et al.
American Journal of Perinatology|March 1, 1994
Aplasia cutis congenita, elevated alpha-fetoprotein, and a distinct amniotic fluid acetylcholinesterase electrophoretic bandY Dror, Z Gelman-Kohan, Z Hagai, et al.
Journal of Medical Genetics|December 1, 1995
Familial café au lait spots: a variant of neurofibromatosis type 1D Abeliovich, Z Gelman-Kohan, S Silverstein, et al.
Pageof 2